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E Ars

Showing results (1-10 of 25) with videos related to

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Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|January 29, 2011
Molecular diagnosis of autosomal dominant polycystic kidney diseaseR Torra Balcells, E Ars Criach
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|April 24, 2003
[Molecular diagnosis of hereditary renal diseases]E Ars, R Torra, A Oliver
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|April 24, 2003
[The Alport syndrome]B Tazón, E Ars, R Torra
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|July 30, 2005
[Collagen IV (alpha3-alpha4) nephropathy]R Torra, B Tazón, E Ars, et al.
Nucleic Acids Research|February 24, 2000
Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNAE Ars, E Serra, S de la Luna, et al.
Prenatal Diagnosis|August 19, 1999
Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutationE Ars, H Kruyer, A Gaona, et al.
Clinical Nephrology|June 10, 2008
Preservation of renal function in a patient with Fabry nephropathy on enzyme replacement therapyR Torra, F Algaba, E Ars, et al.
Nature Genetics|June 30, 2001
Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromasE Serra, T Rosenbaum, M Nadal, et al.
Journal of Medical Genetics|January 15, 2014
Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertilityD Lo Giacco, C Chianese, E Ars, et al.
Human Molecular Genetics|December 23, 1999
Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1E Ars, E Serra, J García, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|January 29, 2011
Molecular diagnosis of autosomal dominant polycystic kidney diseaseR Torra Balcells, E Ars Criach
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|April 24, 2003
[Molecular diagnosis of hereditary renal diseases]E Ars, R Torra, A Oliver
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|April 24, 2003
[The Alport syndrome]B Tazón, E Ars, R Torra
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|July 30, 2005
[Collagen IV (alpha3-alpha4) nephropathy]R Torra, B Tazón, E Ars, et al.
Nucleic Acids Research|February 24, 2000
Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNAE Ars, E Serra, S de la Luna, et al.
Prenatal Diagnosis|August 19, 1999
Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutationE Ars, H Kruyer, A Gaona, et al.
Clinical Nephrology|June 10, 2008
Preservation of renal function in a patient with Fabry nephropathy on enzyme replacement therapyR Torra, F Algaba, E Ars, et al.
Nature Genetics|June 30, 2001
Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromasE Serra, T Rosenbaum, M Nadal, et al.
Journal of Medical Genetics|January 15, 2014
Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertilityD Lo Giacco, C Chianese, E Ars, et al.
Human Molecular Genetics|December 23, 1999
Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1E Ars, E Serra, J García, et al.
Pageof 3